Effects of Dietary Conjugated Linoleic Acid (CLA) on Antioxidant System in the Liver of Chronically Ethanol-Treated Rats

식이에 첨가한 Conjugated Linoleic Acid (CLA)가 만성적으로 알코올을 섭취한 쥐에서 간조직의 항산화 체계에 미치는 영향

  • Kim, Se-Na (Department of Food & Nutrition, Kyung Hee university) ;
  • Kim, Min-Seok (Department of Food & Nutrition, Kyung Hee university) ;
  • Park, Hyun-Suh (Department of Food & Nutrition, Kyung Hee university)
  • 김세나 (경희대학교 생활과학대학 식품영양학과) ;
  • 김민석 (경희대학교 생활과학대학 식품영양학과) ;
  • 박현서 (경희대학교 생활과학대학 식품영양학과)
  • Published : 2007.03.31

Abstract

The study was designed to observe antioxidant activities of conjugated linoleic acid (CLA) by determining antioxidant enzyme protein levels [cytochrome P4502 El (CYP2E1), Copper, Zinc-superoxide dismutase (CuZn-SOD), glutathione peroxidase (CSH-Px), glutathione S-transferase (GST)] by Western blot analysis and the levels of ${\alpha}$-tocopherol and 2-thiobarbituric acid reactive substances (TBARS) in the liver of chronically ethanol-treated rats. Sixty Sprague Dawley male rats were divided into 3 groups (Control, EtOH, EtOH+CLA). All rats were fed Lieber-DeCarli liquid diet for 4 weeks by pair-feeding against the EtOH group. The liquid diet was supplemented with 1.77g CLA mixture per kg diet in the EtOH+CLA group. Isocaloric maltose dextrin was added in replace of 50g ethanol (36%kcal) for the Control group. Ethanol ingestion significantly increased the levels of CYP2E1 protein and TBARS, but significantly reduced CuZn-SOD protein level and increased GST protein level. There was no significant effect on the level of GSH-Px protein and ${\alpha}$-tocopherol in the liver by ethanol. CLA supplementation with ethanol significantly increased the levels of CuZn-SOD, GSH-Px and GST and also significantly attenuated TBARS level, whereas there was no significant effect on the levels of CYP2E1 protein and ${\alpha}$-tocopherol by CLA. Overall, the CLA supplemented to ethanol could significantly increase the levels of CuZn-SOD, GSH-Px and GST proteins and reduce the level of TBARS in the liver of chronically ethanol-treated rats.

Keywords

References

  1. 한국의 사회지표. 서울 통계청, 2004
  2. Lieber CS. Hepatic, metabolic and toxic effects of ethanol: 1991 update. Alcohol Clin Exp Res 15(4): 573-592, 1991 https://doi.org/10.1111/j.1530-0277.1991.tb00563.x
  3. Lieber CS. The influence of alcohol in nutritional status. Nutr Rev 46(7): 241-254, 1988 https://doi.org/10.1111/j.1753-4887.1988.tb05443.x
  4. Purohit V, Brenner DA. Mechanisms of alcohol-induced hepatic fibrosis: a summary of the Rom Thurman Symposium. Hepatology 43(4): 872-878, 2006 https://doi.org/10.1002/hep.21107
  5. Lawrence JC, Jill SG, Eric PD, Joyce AD, Donald DL, Mark AY. Effects of antioxidant treatment of streptozotocin inducd diabetic rats in endonerial blood flow, motor nerve conduction velocity and vascular reactivity of epineurial atterioles of the sciatic nerve. Diabetes 50(8): 1927-1937, 2001 https://doi.org/10.2337/diabetes.50.8.1927
  6. Archer MC. Cancer and diet. Present Knowledge in nutrition 7th ed. ILSI 482-487, 1996-
  7. Ha YL, Strorkson J, Pariza MW. Inhibition of benzo(${\alpha}$)pyreneinduced mouse forestomach neoplasia by conjugated dienoic derivatives of linoleic acid. Cancer Res 50(4): 1097-1101, 1990
  8. Ip C, Scimeca JA, Thompson H. Effect of timing and duration of dietary conjugated linoleic acid on mammary cancer prevention. Nutr Cancer 24(3): 241-247, 1995 https://doi.org/10.1080/01635589509514413
  9. Park Y, Alright KJ, Liu W, Storkson JM, Cook ME, Pariza MW. Effect of conjugated linoleic acid on body composition in mice. Lipids 32(8): 853-858, 1997 https://doi.org/10.1007/s11745-997-0109-x
  10. Lieber CS, DeCarli LM. The feeding of ethanol in liquid diet. Alcohol Clin Exp Res 10(5): 550-553, 1986 https://doi.org/10.1111/j.1530-0277.1986.tb05140.x
  11. Folch J, Lees M, Sloane-Stanley GH. A simple method for the isolation and purification of total lipids from animal tissues. J Bio Chem 226(1): 497-509, 1957
  12. Frings CS, Dunn RT. A colorimetric method for determination of total serum lipids based on the sulfo-phospho-vanillin reaction. Am J Clin Path 53: 89-91, 1970 https://doi.org/10.1093/ajcp/53.1.89
  13. Fletcher MJ. A Colorimetric method for estimating serum triglycerides. Clin Chim Acta 22(3): 393-397, 1968 https://doi.org/10.1016/0009-8981(68)90041-7
  14. Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 95(2): 351-358, 1979 https://doi.org/10.1016/0003-2697(79)90738-3
  15. Desai ID. Vitamin E analysis methods for animal tissues. Method Enzymol 105: 138-147, 1984 https://doi.org/10.1016/S0076-6879(84)05019-9
  16. Bradford MM. A rapid and sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein dye binding. Anal Biochem 72(7): 248-254, 1976 https://doi.org/10.1016/0003-2697(76)90527-3
  17. Mckimm-Breschkim JL. The use of TMB for solid phase immunoassays. J Immunol Methods 135(1-2): 277-280, 1990 https://doi.org/10.1016/0022-1759(90)90282-Z
  18. Rya SY, Kim JH. Effect of chronic alcohol feeding and 2-Acetylaminofluorence treatment on hepatic mitochondrial ATPase activity and membrane lipid composition in rats. J Korean Soc Food Nutr 24(6): 867-873, 1995
  19. Yamada S, Wilson JS, Lieber CS. The effects of ethanol and diet on hepatic and serum ${\gamma}$-glutamyl transpeptidase activities in rats. J Nutr 115(10): 1285-1290, 1985 https://doi.org/10.1093/jn/115.10.1285
  20. Lieber CS, Jones DP, Decarli LM. Effects of prolonged ethanol intake: production of fatty liver despite adequate diets. J Clin Invest 44: 1009-1021, 1965 https://doi.org/10.1172/JCI105200
  21. Lieber CS. Alcoholic fatty liver: its pathogenesis and mechanism of progression to inflammation and fibrisis. Alcohol 34(1): 9-19, 2004 https://doi.org/10.1016/j.alcohol.2004.07.008
  22. Lieber CS. Ethnaol metabolism, cirrhosis and alcoholism. Clin Chim Acta 257(1): 59-84, 1997 https://doi.org/10.1016/S0009-8981(96)06434-0
  23. Seo JS. Alcohol metabolism and nutritional effect. Food Ind Nutr 4(1): 13-19, 1999
  24. Kono H, Bradford BU, Yin M, Sulik KK. Koop DR, Peters JM, Gonzalez FJ, McDonald T, DiKalova A, Kadiiska MB, Mason RP, Thurman RG. CYP2E1 is not involved in early alcohol-induced liver injury. Am J Physiol 277(6): G1259-G1267, 1999
  25. Yun KM, Park HS. Conjugated linoleic acid supplemented to dietary fat has an antioxidant activities, but it depends on the type of fat in diet. Korean J Nutr 34(8): 858-864, 2001
  26. Kessova IG, Ho YS, Thung S, Cederbaum AI. Alcohol-induced liver injury in mice lacking CuZn-superoxide dismutase. Hepatology 38(5): 1136-1145, 2003 https://doi.org/10.1053/jhep.2003.50450
  27. Lee EH, Chyun JH. Effects of ${\beta}-carotene$ supplementation on lipid peroxide levels and antioxidative enzyme activities in alcoholic fatty liver rats. Korean J Nutr 38(5): 289-296, 2005
  28. Zidenberg-Cherr S, Keen CL, Lonnerdal B, Hurley LS. Superoxide dismutase activity an lipid peroxidation in the rat: developmental correlations affected by manganese deficiency. J Nutr 113(12): 2498-2504, 1983 https://doi.org/10.1093/jn/113.12.2498
  29. Hayes JD, Pulford DJ. The glutathione S-transferase supergene family: regulation of GST and the contribution of the isoenzymes to cancer chemoprotection and drug resistance. Crit Rev Biochem Mol Biol 30(6): 445-600, 1995 https://doi.org/10.3109/10409239509083491